Literature DB >> 648543

Chronic mild diarrhoea, stunted growth and neuromuscular abnormalities.

R C Sengers, A M Stadhouders, H H Jaspar, E D Schretlen, P J van Munster.   

Abstract

This report describes a 3 year-old girl with signs of ventricular hypertrophy, short stature, and persistent diarrhoea (without steatorrhoea or creatorrhoea) which was resistant to therapy. There was no clinical evidence of myopathy but a myopathic pattern was found on electromyography. Biochemical studies revealed no abnormalities. Routine histological studies of biopsied muscle showed no obvious structural abnormalities. Examination of 1 micrometer tissue sections revealed groups of atrophic fibers. Electronmicroscopy revealed widened spaces between the myofibrils with disruption of filament arrangement. The mitochondria in the motor end-plates were very distended and almost devoid of cristae.

Entities:  

Mesh:

Year:  1978        PMID: 648543     DOI: 10.1007/BF00442063

Source DB:  PubMed          Journal:  Eur J Pediatr        ISSN: 0340-6199            Impact factor:   3.183


  12 in total

1.  Mitochondrial myopathy with multisystem abnormalities and normal ocular movements.

Authors:  J G McLeod; W de C Baker; C D Shorey; C B Kerr
Journal:  J Neurol Sci       Date:  1975-01       Impact factor: 3.181

2.  Vital staining and electron microscopy of the intramuscular nerve endings in the neuropathy of adult coeliac disease.

Authors:  W T Cooke; A G Johnson; A L Woolf
Journal:  Brain       Date:  1966-12       Impact factor: 13.501

3.  Mitochondrial ultrastructure with crystalloid inclusions in an unusual type of human myopathy.

Authors:  J P Schellens; E Ossentjuk
Journal:  Virchows Arch B Cell Pathol       Date:  1969

4.  A new mitochondrial myopathy in a patient with salt craving.

Authors:  A J Spiro; J W Prineas; C L Moore
Journal:  Arch Neurol       Date:  1970-03

5.  A metabolic myopathy associated with chronic lactic acidemia, growth failure, and nerve deafness.

Authors:  T N Hackett; P F Bray; F A Ziter; W L Nyhan; K M Creer
Journal:  J Pediatr       Date:  1973-09       Impact factor: 4.406

6.  Ophthalmoplegia plus with morphological and chemical studies of cerebellar and muscle tissue.

Authors:  L Schneck; M Adachi; P Briet; A Wolintz; B W Volk
Journal:  J Neurol Sci       Date:  1973-05       Impact factor: 3.181

7.  Chronic lactic acidosis in association with myopathy.

Authors:  M J Terlow; B D Lake; J K Lloyd
Journal:  Arch Dis Child       Date:  1973-06       Impact factor: 3.791

8.  The syndrome of systemic carnitine deficiency. Clinical, morphologic, biochemical, and pathophysiologic features.

Authors:  G Karpati; S Carpenter; A G Engel; G Watters; J Allen; S Rothman; G Klassen; O A Mamer
Journal:  Neurology       Date:  1975-01       Impact factor: 9.910

9.  Skeletal muscle disease with abnormal mitochondria.

Authors:  G K van Wijngaarden; J Bethlem; A E Meijer; W C Hülsmann; C A Feltkamp
Journal:  Brain       Date:  1967-09       Impact factor: 13.501

10.  Cardiomyopathy and short stature associated with mitochondrial and/or lipid storage myopathy of skeletal muscle.

Authors:  R C Sengers; A M Stadhouders; H H Jaspar; J M Trijbels; O Daniels
Journal:  Neuropadiatrie       Date:  1976-05
View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.